| Gene Information | |
|---|---|
| Gene Name | C13orf2 |
| Organism | Homo sapiens (Human) |
| Gene Length | 325 |
| Protein Names | BTB/POZ domain-containing protein KCTD12 (Pfetin) (Predominantly fetal expressed T1 domain) |
| Target Name | NA |
| Target Type | NA |
| Gene Age | NA |
| Evolutionary Stage | NA |
| AlphaFoldDB | Q96CX2 |
| Gene Card | KCTD12 |
| Uniprot ID | Q96CX2 |
| Pfam | PF02214 |
| In ASD | no |
| Allosteric Prediction | NA |
| Ortholog in Animals | NA |
| Ohnologs | NA |
| Paralogs | NA |
| Tissue | NA |
| Tissue Specificity | Present in a variety of fetal organs, with highest expression levels in the cochlea and brain and, in stark contrast, is detected only at extremely low levels in adult organs, such as brain and lung. {ECO:0000269|PubMed:15357420}. |
| Pharmacological Animal Models | NULL(Chimpanzee);0.001000(Mouse);NULL(Rat);0.066667(Rabbit) |
| Gene Ontology (biological process) |
|
| Gene Ontology (cellular component) |
|
| Gene Ontology (molecular function) |
|
| PDB | 6M8S (X-ray 3.71A ) 6QZL (X-ray 1.98A ) |
| DBSNP | NA |
| Subcellular location [CC] | Presynaptic cell membrane. Postsynaptic cell membrane {ECO:0000250}. |
| Mouse PG classification | NA |
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